Literature DB >> 31270084

A rare case of hyperammonaemic encephalopathy.

Yeu Jye Pang1, Stephanie Day1, Daniel Sumner2, Kenneth Adegoke1.   

Abstract

A 75-year-old female patient presented to the accident and emergency department following a collapse. She was treated for a saddle pulmonary embolism and underlying urinary tract infection. However, 48 hours later she was found to have reduced consciousness with no apparent cause (Glasgow Coma Scale of 8 out of 15). Subsequent blood results revealed a highammonia level. After reflection into her medical history, it was found that she had bladder exstrophy, which was managed with urinary diversion surgery as an infant, and her presentation was a rare complication of this operation. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  congenital disorders; surgery; urological surgery

Mesh:

Substances:

Year:  2019        PMID: 31270084      PMCID: PMC6613968          DOI: 10.1136/bcr-2018-228410

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  4 in total

Review 1.  Severe hyperammonaemia in adults not explained by liver disease.

Authors:  Valerie Walker
Journal:  Ann Clin Biochem       Date:  2012-02-20       Impact factor: 2.057

2.  Rifaximin treatment for reduction of risk of overt hepatic encephalopathy recurrence.

Authors:  Steven L Flamm
Journal:  Therap Adv Gastroenterol       Date:  2011-05       Impact factor: 4.409

3.  Intermittent hyperammonemic encephalopathy after ureterosigmoidostomy: spontaneous onset in the absence of hepatic failure.

Authors:  Wolfgang Jäger; Anne-Odette Viertmann; Claudia Janßen; Frank Birklein; Joachim W Thüroff; Raimund Stein
Journal:  Cent European J Urol       Date:  2015-03-13

4.  Metabolic complications of urinary intestinal diversion.

Authors:  Nikhil Vasdev; Andrew Moon; Andrew C Thorpe
Journal:  Indian J Urol       Date:  2013-10
  4 in total

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